Literature DB >> 3010595

Coronavirus IBV: partial amino terminal sequencing of spike polypeptide S2 identifies the sequence Arg-Arg-Phe-Arg-Arg at the cleavage site of the spike precursor propolypeptide of IBV strains Beaudette and M41.

D Cavanagh, P J Davis, D J Pappin, M M Binns, M E Boursnell, T D Brown.   

Abstract

The spike protein of avian infectious bronchitis coronavirus comprises two glycopolypeptides S1 and S2 derived by cleavage of a proglycopolypeptide So, the nucleotide sequence of which has recently been determined for the Beaudette strain (Binns, M.M. et al., 1985, J. Gen. Virol. 66, 719-726). The order of the two glycopolypeptides within So is aminoterminus(N)-S1-S2-carboxyterminus(C). To locate the N-terminus of S2 we have performed partial amino acid sequencing on S2 from IBV-Beaudette labelled with [3H]serine and from the related strain labelled with [3H]valine, leucine and isoleucine. The residues identified and their positions relative to the N-terminus of S2 were: serine, 13; valine, 6, 12; leucine, none in the first 20 residues; isoleucine, 2, 19. These results identified the N-terminus of S2 of IBV-Beaudette as serine, 520 residues from the N-terminus of S1, excluding the signal sequence. Immediately to the N-terminal side of residue 520 So has the sequence Arg-Arg-Phe-Arg-Arg; similar basic connecting peptides are a feature of several other virus spike glycoproteins. It was deduced that for IBV-Beaudette S1 comprises 519 residues (Mr 57.0K) or 514 residues (56.2K) if the connecting peptide was to be removed by carboxypeptidase-like activity in vivo while S2 has 625 residues (69.2K). Nucleotide sequencing of the cleavage region of the So gene of IBV-M41 revealed the same connecting peptide as IBV-Beaudette and that the first 20 N-terminal residues of S2 of IBV-M41 were identical to those of the Beaudette strain. IBV-Beaudette grown in Vero cells had some uncleaved So; this was cleavable by 10 micrograms/ml of trypsin and of chymotrypsin. Partial N-terminal analysis of S1 from IBV-M41 identified leucine and valine residues at positions 2 and 9 respectively from the N-terminus. This confirms the identification, made by Binns et al. (1985), of the N-terminus of S1 and the end of the signal sequence of the IBV-Beaudette spike propolypeptide. N-terminal sequencing of [3H]leucine-labelled IBV-Beaudette membrane (M) polypeptide showed leucine residues at positions 8, 16 and 22 from the N-terminus; these results confirm the open reading frame identified by M.E.G. Boursnell et al. (1984, Virus Res. 1, 303-313) in the nucleotide sequence of M. The N-terminus of the nucleocapsid (N) polypeptide appeared to be blocked.

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Year:  1986        PMID: 3010595      PMCID: PMC7133853          DOI: 10.1016/0168-1702(86)90037-7

Source DB:  PubMed          Journal:  Virus Res        ISSN: 0168-1702            Impact factor:   3.303


  32 in total

1.  Purification of the fusion protein of Sendai virus: analysis of the NH2-terminal sequence generated during precursor activation.

Authors:  M J Gething; J M White; M D Waterfield
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2.  Aminopropyl glass and its p-phenylene diisothiocyanate derivative, a new support in solid-phase Edman degradation of peptides and proteins.

Authors:  E Wachter; W Machleidt; H Hofner; J Otto
Journal:  FEBS Lett       Date:  1973-09-01       Impact factor: 4.124

3.  The structure of the hemagglutinin, a determinant for the pathogenicity of influenza viruses.

Authors:  F X Bosch; M Orlich; H D Klenk; R Rott
Journal:  Virology       Date:  1979-05       Impact factor: 3.616

4.  Proteolytic cleavage of peplomeric glycoprotein E2 of MHV yields two 90K subunits and activates cell fusion.

Authors:  L S Sturman; K V Holmes
Journal:  Adv Exp Med Biol       Date:  1984       Impact factor: 2.622

Review 5.  Cotranslational and posttranslational processing of viral glycoproteins.

Authors:  H D Klenk; R Rott
Journal:  Curr Top Microbiol Immunol       Date:  1980       Impact factor: 4.291

6.  Buffer gradient gels and 35S label as an aid to rapid DNA sequence determination.

Authors:  M D Biggin; T J Gibson; G F Hong
Journal:  Proc Natl Acad Sci U S A       Date:  1983-07       Impact factor: 11.205

7.  Cloning and sequencing of the gene encoding the spike protein of the coronavirus IBV.

Authors:  M M Binns; M E Boursnell; D Cavanagh; D J Pappin; T D Brown
Journal:  J Gen Virol       Date:  1985-04       Impact factor: 3.891

8.  Studies on the primary structure of the influenza virus hemagglutinin.

Authors:  J J Skehel; M D Waterfield
Journal:  Proc Natl Acad Sci U S A       Date:  1975-01       Impact factor: 11.205

9.  Structural polypeptides of coronavirus IBV.

Authors:  D Cavanagh
Journal:  J Gen Virol       Date:  1981-03       Impact factor: 3.891

10.  Characterization of coronavirus II. Glycoproteins of the viral envelope: tryptic peptide analysis.

Authors:  L S Sturman; K V Holmes
Journal:  Virology       Date:  1977-04       Impact factor: 3.616

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  67 in total

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3.  Reverse genetics system for the avian coronavirus infectious bronchitis virus.

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5.  Bovine torovirus: sequencing of the structural genes and expression of the nucleocapsid protein of Breda virus.

Authors:  L M Duckmanton; R Tellier; P Liu; M Petric
Journal:  Virus Res       Date:  1998-11       Impact factor: 3.303

6.  The spike protein of infectious bronchitis virus is retained intracellularly by a tyrosine motif.

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7.  Acquisition of cell-cell fusion activity by amino acid substitutions in spike protein determines the infectivity of a coronavirus in cultured cells.

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Journal:  PLoS One       Date:  2009-07-02       Impact factor: 3.240

8.  Sequence analysis of the S1 glycoprotein gene of infectious bronchitis viruses: identification of a novel phylogenetic group in Korea.

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9.  Detection and molecular characterization of infectious bronchitis virus isolated from recent outbreaks in broiler flocks in Thailand.

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10.  The replicase gene of avian coronavirus infectious bronchitis virus is a determinant of pathogenicity.

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Journal:  PLoS One       Date:  2009-10-09       Impact factor: 3.240

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